A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6532247



Internal ID9459840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1664580..1666986hg38UCSC Ensembl
Outerchr7:1664209..1667356hg38UCSC Ensembl
Innerchr7:1704216..1706622hg19UCSC Ensembl
Outerchr7:1703845..1706992hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg383148
hg193148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672578
Supporting Variants
SamplesNA18910
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6532247
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer